Hip implant Recall: Howmedica Osteonics TRI TS BASEPLATE SIZE 3
Announced 2026-06-24 · FDA
This recall involves Exeter V40 stems (0580-1-442, lot A00976) and (0580-1-352, lot G8754849) distributed internationally in the United Kingdom. It concerns a potential mix-up between catalog numbers that could affect patient labeling. Fifty-five units were distributed outside the United States.
| Brand | Howmedica Osteonics Corp. |
|---|---|
| Product | 1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352; |
| Reason | a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted. |
| Severity | moderate |
| Units affected | 7 |
| Distribution | International distribution in the country of United Kingdom. |
| Agency | FDA |
| Recall / campaign no. | 1. Model/Catalog Number: 0580-1-442, UDI-DI: 04546540153319, Lot Number: A00976; 2. Model/Catalog Number: 0580-1-352, UDI-DI: 04546540153241, Lot Number: G8754849; |
WHAT YOU SHOULD DO
- If you have an Exeter V40 stem with catalog 0580-1-442 or 0580-1-352, check your lot numbers A00976 or G8754849 to determine if your device could be affected.
- Contact your orthopedic surgeon or hospital to discuss whether your device is involved and what action is required.
- Do not attempt to modify or remove the implant yourself; follow the guidance provided by your surgeon or the hospital.
- Keep records of implant details; report any symptoms or concerns to your healthcare provider and follow their instructions.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.